机译:临床环境中的exome测序:稀有疾病患儿父母的偏好和经验(续集研究)
Univ Burgundy Franche Comte EA3189 Lab Sociol &
Anthropol LaSA Besancon France;
Univ Burgundy Franche Comte FHU TRANSLAD Dijon France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
CHRU Besancon Inserm 1431 Clin Invest Ctr Besancon France;
Dijon Univ Hosp Ctr Reference Anomalies Dev &
Syndromes Malformat Dijon France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
Univ Burgundy Franche Comte EA3189 Lab Sociol &
Anthropol LaSA Besancon France;
Univ Burgundy Franche Comte FHU TRANSLAD Dijon France;
Dijon Univ Hosp Ctr Reference Anomalies Dev &
Syndromes Malformat Dijon France;
Dijon Univ Hosp Ctr Reference Anomalies Dev &
Syndromes Malformat Dijon France;
Dijon Univ Hosp Ctr Reference Anomalies Dev &
Syndromes Malformat Dijon France;
Dijon Univ Hosp Ctr Reference Anomalies Dev &
Syndromes Malformat Dijon France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
Univ Burgundy Franche Comte FHU TRANSLAD Dijon France;
Univ Burgundy Franche Comte FHU TRANSLAD Dijon France;
Dijon Univ Hosp Ctr Reference Anomalies Dev &
Syndromes Malformat Dijon France;
Dijon Univ Hosp Ctr Reference Anomalies Dev &
Syndromes Malformat Dijon France;
Univ Strasbourg SuLiSoM EA 3071 Strasbourg France;
Univ Burgundy Franche Comte Dijon UMR 7366 Ctr Georges Chevrier Dijon France;
Alliance Malad Rares Paris France;
Alliance Malad Rares Paris France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
Ctr Reference Anomalies Dev &
Syndromes Malformat Serv Genet Clin Lyon France;
Univ Burgundy Franche Comte EA7467 Lab Econ Dijon LEDI Dijon France;
Univ Burgundy Franche Comte EA7467 Lab Econ Dijon LEDI Dijon France;
Univ Burgundy Franche Comte FHU TRANSLAD Dijon France;
机译:临床环境中的exome测序:稀有疾病患儿父母的偏好和经验(续集研究)
机译:临床exome测序,一种检测罕见疾病致病性突变的有效工具:过去七年的回顾性研究
机译:在产前和围产期期间鉴定患有痛经时的父母经验和偏好:对家庭护理治疗稀有疾病的定性研究
机译:在临床医学实验室中通过外显子组测序建立与基因有关的罕见病报告格式
机译:使用全基因组测序发现导致罕见的小儿肾脏疾病的新基因
机译:临床环境中的外显子组测序:罕见疾病患儿父母的偏好和经历(SEQUAPRE研究)
机译:导航稀有疾病的儿童的美国健康保险景观:对父母经验的定性研究。